MDR TB treatment in prison

A. Pasechnikov, J. Mucherjee, S. Shin, M. Rich, O. Kostornoy, S. Mishustin, Y. Karpeichik, S. Faraphonov, O. Kosogorova (Boston, United States Of America; Tomsk, Russia)

Source: Annual Congress 2002 - Drug resistance
Session: Drug resistance
Session type: Poster Discussion
Number: 3839
Disease area: Respiratory infections

Congress or journal article abstract

Abstract

40 MDR TB chronic patients were treated for 18 month with capreomycin (kanamycine), cycloserine, ofloxacine, PAS and ethambutol, pyrazinamide and ethionamide, if susceptibility was persisted. The average number of drugs used in treatment regimens was 5. 100% were resistant to isoniazid, rifampin and streptomycin, 95% - to etambutol, 32% - to kanamycin, 34% - to ethionamide and 49% - to pirazinamide. 15 were smear and 29 culture positive, both positive were 30 patients (75%). All others were positive 3-7 month before start of treatment and had x-ray signs of TB activity. At the first 2-3 month most often the different gastrointestinal disturbances occurred: diarrhea (63%), nausea (66%), vomiting (42%), reflux (53%), abdomen pain(45%),appetite decreasing (45%) and swelling(11%). Severe psychiatric disorders have occurred after 4 month: 5 patients had acute psychoses and one had convulsions simultaneously; 7 patients had depression. After 3 month 5 patients had severe potassium deficit and decreasing its level below 2.0 mEq. After 9 month in 45% cases hypothyroid syndrome have developed. One patient had hepatitis connected with Z using. In 6 cases episodically we saw transaminases elevating up to 5 folders without disease developing. Usually we did not stop treatment, except severe side effects cases, when we have interruption for 1-2 weeks. Smear and culture conversion registered at 6-7 month of 93%. Bacteriology changes correlated with TB complaints reducingand X-ray positive changes. One patient died of acute coronary insufficient and widespread atherosclerosis. One another died after surgical operation because of TB progress. One patient operated successfully.


Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
A. Pasechnikov, J. Mucherjee, S. Shin, M. Rich, O. Kostornoy, S. Mishustin, Y. Karpeichik, S. Faraphonov, O. Kosogorova (Boston, United States Of America; Tomsk, Russia). MDR TB treatment in prison. Eur Respir J 2002; 20: Suppl. 38, 3839

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
MDR-TB treatment in prison setting
Source: Annual Congress 2007 - Tuberculosis control in the penitentiary and civilian sector
Year: 2007


Linezolid in the treatment of patients with MDR TB and XDR TB
Source: Annual Congress 2013 –Drug-resistant tuberculosis
Year: 2013


Our experience in multi drug resistant tuberculosis (MDR TB) treatment
Source: Eur Respir J 2005; 26: Suppl. 49, 652s
Year: 2005

MDR-TB and XDR-TB: drug resistance and treatment outcomes
Source: Eur Respir J 2009; 34: 778
Year: 2009


Collapsotherapy of multi-drug resistant TB in prisoners
Source: Eur Respir J 2003; 22: Suppl. 45, 522s
Year: 2003

Is prevalence of MDR TB and XDR TB decreasing in a tertiary care hospital in India?
Source: International Congress 2017 – MDRTB: detection and management
Year: 2017


Prevalence of MDR TB and XDR TB in a tertiary care hospital in India
Source: Annual Congress 2008 - Clinical epidemiology of tuberculosis
Year: 2008


Surgical treatment for MDR TB patients – preliminary results from a Romanian MDR TB centre
Source: Eur Respir J 2006; 28: Suppl. 50, 276s
Year: 2006

Is standardized treatment appropriate for non-XDR multiple drug resistant TB?
Source: Annual Congress 2008 - Epidemiology and clinical management of multidrug-resistant and extensively drug-resistant tuberculosis
Year: 2008

Who is responsible for MDR- TB?
Source: International Congress 2015 – WHO guidelines in TB and clinical practice
Year: 2015


Efficacy of treatment in MDR and XDR lung TB patients in the follow-up period with the use of new anti-tuberculosis agent
Source: International Congress 2019 – Extra-pulmonary tuberculosis and comorbidities
Year: 2019

Why did they get XDR TB ?
Source: Annual Congress 2011 - Risk factors and treatment outcomes in multidrug- and extensively drug-resistant tuberculosis
Year: 2011


Surgical treatment of multidrug-resistant tuberculosis (MDR TB)
Source: Eur Respir J 2003; 22: Suppl. 45, 523s
Year: 2003

Spread of tuberculosis among household contacts of multi drug resistant tuberculosis (MDRTB) patients
Source: International Congress 2014 – Tuberculosis: epidemiology and public health
Year: 2014


Effectiveness of the WHO regimen for treatment of multidrug resistant tuberculosis (MDR-TB)
Source: Annual Congress 2013 –Drug-resistant tuberculosis: new clinical and public health insights
Year: 2013

Multidrug resistant tuberculosis (MDR – TB) treatment outcomes in Iran
Source: Eur Respir J 2004; 24: Suppl. 48, 657s
Year: 2004

Prevalence of MDR and XDR tuberculosis among patients with failure of re-treatment course
Source: Annual Congress 2008 - The challenge of multidrug-resistant tuberculosis
Year: 2008

The depressive syndrome as a response to the TB treatment in MDR TB patients
Source: Annual Congress 2008 - Clinical epidemiology of tuberculosis III
Year: 2008

Second and third line anti-tuberculosis drug's side effects during the treatment of patients with multidrug resistant tuberculosis (MDR TB)
Source: Eur Respir J 2003; 22: Suppl. 45, 555s
Year: 2003

Frequency of risk factors for multi-drug resistant tuberculosis among the patients enrolled at multi-drug resistant clinic in a tertiary care hospital, Pakistan
Source: International Congress 2014 – Tuberculosis: from epidemiology to therapy 1
Year: 2014